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Radial Jaw 4

FDA UDI

Class I (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Radial Jaw 4 FDA UDI
Generic Name
Flexible endoscopic biopsy forceps, single-use FDA UDI
Device Name
Single-Use Biopsy Forceps FDA UDI
Model / Reference
M00513400 FDA UDI
Description
Single-Use Biopsy Forceps FDA UDI

Identifiers

Primary DI / UDI-DI
08714729745662 FDA UDI
FDA Product Code
FCL FDA UDI
GMDN Term
Flexible endoscopic biopsy forceps, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1075 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Flexible endoscopic biopsy forceps, single-use

Radial Jaw 4 by Boston Scientific — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI b3fdec72-d3f0-4970-9d22-64b49c615e8b 34 fields · synced Jun 8, 2026